A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14214979



Internal ID3152264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77610862..77622595hg38UCSC Ensembl
Innerchr11:77610862..77622595hg38UCSC Ensembl
Outerchr11:77610362..77623095hg38UCSC Ensembl
chr11:77321907..77333640hg19UCSC Ensembl
Innerchr11:77321907..77333640hg19UCSC Ensembl
Outerchr11:77321407..77334140hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3811734
hg1911734
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626888
Supporting Variants
SamplesHG02775
Known GenesCLNS1A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14214979
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer